IRRADIATION DEVICE FOR BIOLOGICAL FLUIDS

Abstract

A device for irradiation of a biological product/substance is provided comprising a base; a tray having a first and second side associated with the base and configured to receive a container holding the biological product/substance to be irradiated; a first array of radiation-emitting bulbs mounted in the device adjacent the first side of the tray; a second array of radiation-emitting bulbs mounted in device adjacent a second side of the tray; a first filter mounted in the device between the tray and the first array of radiation-emitting bulbs for blocking and/or reflecting radiation emitted by the first array of a selected wavelength; and a second filter mounted in the device beneath the second array of radiation-emitting bulbs for blocking and/or reflecting radiation emitted by the second array of the selected wavelength.

Claims

1. A device for irradiation of a biological product/substance comprising: a) a base; b) a tray having a first and second side associated with the base and configured to receive a container holding the biological product/substance to be irradiated; c) a first array of radiation-emitting bulbs mounted in the device adjacent the first side of the tray; d) a second array of radiation-emitting bulbs mounted in device adjacent the second side of the tray; e) a first filter mounted in the device between the tray and the first array of radiation-emitting bulbs for blocking and/or reflecting radiation emitted by the first array of a selected wavelength; and f) a second filter mounted in the device between the tray and the second array of radiation-emitting bulbs for blocking and/or reflecting radiation emitted by the second array of the selected wavelength; g) each of the first and second filters comprising a substrate having a first surface facing toward the tray and a second surface facing away from the tray and toward its associated array of radiation-emitting bulbs, the second surface of each substrate having a coating thereon for blocking and/or reflecting radiation of the selected wavelength.

2. The device of claim 1 wherein the first and second filters each blocks and/or reflects infrared (IR) radiation while permitting ultraviolet (UV) radiation to pass therethrough.

3. (canceled)

4. The device of claim 2 wherein the substrate comprises glass and the coating comprises silver.

5. The device of claim 4 wherein the coating has a thickness of from 0.5 m to 1.0 m.

6. The device of claim 5 wherein the substrate has a thickness of from 3.3 mm.sup.+/1.3 mm.

7. The device of claim 1 further comprising a fan mounted within the base, the base including vents to permit air circulation and exchange around the tray.

8. The device of claim 7 further comprising a sensor for measuring the radiant output of the radiation-emitting bulbs and a controller configured to adjust the speed of the fan based on a signal received from the sensor to vary the radiant output of the radiation-emitting bulbs.

9. A system for irradiating a biological product/substance comprising: a) a container for holding the biological product/substance to be irradiated; b) an irradiation device comprising: i) a base; ii) an openable cover; iii) a tray associated with the base configured to receive the container of the biological product/substance to be irradiated; iv) a first array of radiation-emitting bulbs mounted in the base beneath the tray; v) a second array of radiation-emitting bulbs mounted in the cover; vi) a first filter mounted in the base between the tray and the first array of radiation-emitting bulbs for blocking and/or reflecting radiation emitted by the first array of a selected wavelength; and vii) a second filter mounted in the cover between the tray and the second array of radiation-emitting bulbs for blocking and/or reflecting radiation emitted by the second array of the selected wavelength; viii) each of the first and second filters comprising a substrate having a first surface facing toward the tray and a second surface facing away from the tray and toward its associated array of radiation-emitting bulbs, the second surface of each substrate having a coating thereon for blocking and/or reflecting radiation of the selected wavelength.

10) The device of claim 9 wherein the first and second filters each blocks and/or reflects infrared (IR) radiation while permitting ultraviolet (UV) radiation to pass therethrough.

11) (canceled)

12) The device of claim 10 wherein the substrate comprises glass and the coating comprises silver.

13) The device of claim 12 wherein the coating has a thickness of from 0.5 m to 1.0 m.

14) The device of claim 13 wherein the substrate has a thickness of from 3.3 mm.sup.+/1.3 mm.

15) The device of claim 9 further comprising a fan mounted within the base, the base including vents to permit air circulation and exchange around the tray.

16) The device of claim 15 further comprising a sensor for measuring the radiant output of the radiation-emitting bulbs and a controller configured to adjust the speed of the fan based on a signal received from the sensor to vary the radiant output of the radiation-emitting bulbs.

17) A method for irradiating a mononuclear cell product comprising: a) placing a collection container suitable for irradiation into an irradiation chamber defined by an exterior surface having a coating thereon that blocks and/or reflects non-UVA light, the irradiation chamber being positioned between first and second light sources; b) introducing a suspension comprising mononuclear cells into the collection container; c) activating the first and second light sources to introduce UVA light into the irradiation chamber to expose the collection container to UVA light; d) preventing non-UVA light from entering into the collection chamber; e) measuring a radiant output of the first and second light sources; f) comparing the measured radiant output to a maximum radiant output for the light sources; and g) varying a speed of a fan associated with the irradiation chamber to selectively increase or decrease the temperature of the light sources to vary the radiant output thereof.

18) (canceled)

19) The method of claim 17 wherein the speed of the fan is increased to decrease the temperature of the light sources.

20) The method of claim 17 wherein the speed of the fan is decreased to increase the temperature of the light sources.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0019] FIG. 1 is a perspective view of an irradiation device for biological fluids in accordance with the present disclosure.

[0020] FIG. 2 is a perspective view, in cross section, of the irradiation device of FIG. 1.

[0021] FIG. 3 is a fragmentary cross sectional view of the irradiation device of FIG. 1, enlarged to show detail.

[0022] FIG. 4 is a perspective view, in cross section, of a tray for supporting a biological fluid container that forms a part of the irradiation device.

[0023] FIG. 5 is a schematic view of a microprocessor-based control system for adjusting the speed of a fan associated with the irradiation device.

DESCRIPTION OF THE ILLUSTRATED EMBODIMENTS

[0024] The embodiments disclosed herein are for the purpose of providing an exemplary description of the present subject matter. They are, however, only exemplary, and the present subject matter may be embodied in various forms. Therefore, specific details disclosed herein are not to be interpreted as limiting the subject matter as defined in the accompanying claims.

[0025] As described herein, the irradiation device is a stand-alone device that may also be used in conjunction with a cell separator as part of a system. According to such a system, the cell separator would be configured to direct a biological fluid into a biological fluid container, and the irradiation device would include a fluid treatment chamber configured to receive the biological fluid container.

[0026] The cell separator may be an Amicus Separator made and sold by Fenwal, Inc., of Lake Zurich, Ill., a subsidiary of Fresenius Kabi USA, LLC. Mononuclear cell collections using a device such as the Amicus are described in greater detail in U.S. Pat. No. 6,027,657, the contents of which is incorporated by reference herein in its entirety.

[0027] The container may be part of a fluid circuit (also referred to as a processing set) that includes a network of tubing and pre-connected containers for establishing flow communication with the patient and for processing and collecting fluids and blood and blood components.

[0028] An exemplary fluid circuit is disclosed in US 2013/0197419, incorporated herein by reference. As disclosed therein, the fluid circuit includes a separation chamber defined by the walls of a flexible processing container, as well as a container for supplying anticoagulant, a waste container for collecting waste from one or more steps in the process for treating and washing mononuclear cells, a container for holding saline or other wash or resuspension medium, a container for collecting plasma, a container for collecting the mononuclear cells from the operation discussed above and, optionally, a container for holding a photoactivation agent.

[0029] The mononuclear cell collection container may also serve as the illumination or irradiation container, and is preferably pre-attached to the disposable set. The fluid circuit includes an inlet line, an anticoagulant (AC) line for delivering AC from the AC container, an RBC line for conveying red blood cells from the separation chamber to a waste container, a platelet-poor plasma (PPP) line for conveying PPP to plasma container, and a line for conveying mononuclear cells between the separation chamber and the collection/illumination container. The blood processing set also includes one or more venipuncture needle(s) for accessing the circulatory system of the patient. The fluid circuit may include both an inlet needle and a return needle. Alternatively, a single needle can serve as both the inlet and return needle.

[0030] The mononuclear cell collection container is suitable for irradiation by light of a selected wavelength. By suitable for irradiation, it is meant that the walls of the container are sufficiently translucent to light of the selected wavelength. In treatments using UVA light, for example, container walls made of ethylene vinyl acetate (EVA) are suitable. Accordingly, the container in which the mononuclear cells are collected may serve both as the collection container and the irradiation container. The collection/irradiation container may be placed inside the irradiation device by the operator or, more preferably, may be placed inside the irradiation chamber of irradiation device at the beginning of a procedure including the cell separator and prior to whole blood withdrawal. In any event, the mononuclear cell collection container preferably remains integrally connected to the remainder of the fluid circuit during the entire procedure, thereby maintaining the closed or functionally closed condition of the fluid circuit. Fluid flow through fluid circuit is preferably driven, controlled and adjusted by a microprocessor-based controller in cooperation with the valves, pumps, weight scales and sensors of the separation device and fluid circuit, the details of which are described in U.S. Pat. No. 6,027,657, referenced above.

[0031] Turning to FIGS. 1-4, an irradiation device, generally designated 10, is seen that comprises a housing 12 including a base 14 and a cover or closure 16. As illustrated, the cover is secured to the base 14 by a hinge so that the cover 16 can be pivoted about the hinge to provide access to the interior of the housing 12. The interior of the housing defines a fluid treatment chamber that includes a tray 18 configured to receive and support a biological fluid container 20.

[0032] The tray 18 has opposed first and second sides, one facing the base 14 and the other facing the cover 16. The tray 18 may be made, in part, of a polymeric material, with certain sections of the tray being made of another material, such as glass.

[0033] A light source is disposed on the interior of the device adjacent each of the first and second sides of the tray. As illustrated, the light source includes a first array 22, including a plurality of light sources 22a, mounted in the base on the first side of the tray, and a second array 24, including a plurality of light sources 24a, mounted in the cover 16 on the second side of the tray 18. According to the present disclosure, the light sources 22a, 24a provide electromagnetic radiation in the ultraviolet portion of the spectrum.

[0034] The treatment chamber is defined by a translucent ceiling 26 and a translucent floor 28 that are interposed between the tray 18 and the upper and lower arrays of light sources, 24a, 22a, respectively, to permit the illumination on both sides of the biological fluid container 20. The floor 28 and ceiling 26 may be made of, e.g., glass. As illustrated, the glass sheets forming the floor and ceiling are mounted in a frame 30 (best seen in FIGS. 3 and 4) that is attached or secured to, or formed integrally with, the interior of the housing 12, e.g., the base 14 or tray 18 and the cover 16.

[0035] The translucent ceiling 26 and floor 28 preferably serve as filters that permit passage of light of the spectrum/wavelength required for treatment of the biological fluid (e.g., activation of a photoactive agent in the biological fluid), but block light outside of the desired spectrum/wavelength, so as to avoid heating of the contents of the treatment container other than that incidental to the absorption of light of the desired spectrum. In the context of the treatment of mononuclear cells, the desired spectrum is UV light having a wavelength in the UVA range of about 320 nm to 400 nm, while the light to be blocked is light falling outside the UVA range, and more specifically, IR light having a wavelength of from about 750 nm to 1 mm.

[0036] In keeping with the disclosure, each of the translucent floor 28 and ceiling 26 comprises a first surface facing the tray 18 and a second surface 28a, 26a (best seen in FIG. 3), facing away from the tray 18 and toward its associated array of radiation-emitting bulbs 22a, 24a. The second surface 28a, 26a, of each of the floor 28 and ceiling 26, i.e., that surface facing away from the tray 18, has a coating thereon for blocking and/or reflecting radiation of the selected wavelength. This helps to reflect the undesirable light (e.g., IR) away from the floor and ceiling before being absorbed, and thus prevents warming of the floor and ceiling.

[0037] Each of the floor 28 and the ceiling 26 comprises a substrate with a coating thereon for blocking and/or reflecting radiation of the selected wavelength. As noted above the floor and ceiling comprise glass, which provides the substrate and the coating comprises silver. The coating preferably has a thickness of from 0.5 m to 1.0 m. The substrate should have a thickness that is not so great as to block UV light, but not so thin as to be unduly prone to breaking. Accordingly, the substrate preferably has a thickness of 3.3 mm.sup.+/1.3 mm. Glass plates having such characteristics will transmit UV light having a wavelength of 320-400 nm, while blocking IR light having a wave length of 750 nm-1 mm, and may be obtained from, e.g., Shott North America, Inc. of Duryea, Pa., under the product designation B-270.

[0038] In order to further moderate the temperature of the treatment chamber, the device preferably includes a fan or blower 32 mounted within the base, and the base includes vents 34 to permit air circulation and exchange around the tray. Further, the speed of the fan 32 is preferably controllable to vary the UVA output of the light sources 22a, 24a. Specifically, the radiant output of the light sources varies with temperature, with the radiant output increasing to a maximum as the temperature of the light sources approaches 40 C. (at the tube wall) and then decreasing. Thus, the UVA output of the light sources may be increased to or decreased from a maximum value by controlling the temperature of the light sources, which can be accomplished by varying the rate of air flow through the irradiation device 10 by increasing the fan speed (to decrease the temperature of the light sources) or decreasing the fan speed (to increase the temperature of the light sources).

[0039] To this end, and with reference to FIG. 5, a UVA sensor 34 is mounted on the interior the compartments for the light sources 22a, 24a in proximity to the light sources. The sensor(s) 34 generate a signal indicative of the radiant output of the light sources that is transmitted to a programmable controller 36. The programmable controller 36 compares the signal from the UVA sensor(s) 34 to a rated maximum radiant output for the light sources, and then controls the speed of the fan 32 to either increase or decrease the ambient temperature of the light sources to adjust the radiant output of the light sources. For example, maximizing the UVA output of the light sources 22a, 24a would shorten the time of irradiation of the fluid container 20.

[0040] By way of example, a description of the use of the irradiation device described herein for the treatment of mononuclear cells with ultraviolet light follows. In such a treatment method, whole blood is withdrawn from a patient and introduced into the separation chamber of the cell separator, where the whole blood is subjected to a centrifugal field. The centrifugal field separates the target cell population, i.e., mononuclear cells, from red blood cells, platelets and plasma. The separated red blood cells and platelets may be returned to the patient, or may be diverted to a container for further processing. However, a residual quantity of red blood cells and plasma typically remains in suspension with the separated mononuclear cells.

[0041] The suspended mononuclear cells may be combined with a lysing agent and then incubated to activate the lysing agent to disintegrate or dissolve the residual red blood cells. The suspension is then washed with the apheresis device to remove plasma and hemoglobin freed by the lysis of the red blood cells. The washed, lysed suspension is then re-suspended, and combined with an activation agent, and then exposed to ultraviolet light to obtain a treated cell product. In one non-limiting example, during treatment, the mononuclear cell product may be exposed to UV bulbs having a wavelength in the UVA range of about 320 nm to 400 nm for a selected period of time, preferably 5 minutes or less, resulting in an average UVA exposure of approximately 0.5-5.0 J/cm2. Due to the IR reflective/blocking coating on the floor and ceiling that define the treatment chamber, the UVA light needed for treating the mononuclear cell product passes into the treatment chamber, while the undesirable IR light is reflected away, thus avoiding heating of the mononuclear cell product that would have otherwise resulted due to its absorption of the IR light.

[0042] The treated cell product is then returned to the patient. Optionally, the treated mononuclear cells may first be returned to separator and concentrated to provide for the concentrated cells to have a smaller total volume as compared to un-concentrated cells. As a result, the smaller volume of concentrated MNCs may be more quickly reinfused to a patient.

[0043] It will be understood that the embodiments described above are illustrative of some of the applications of the principles of the present subject matter. Numerous modifications may be made by those skilled in the art without departing from the spirit and scope of the claimed subject matter, including those combinations of features that are individually disclosed or claimed herein. For these reasons, the scope hereof is not limited to the above description, but is set forth in the following claims.